| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8248042-8248119 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249207-8249331 | Common:1; Rare:37 | ||||
| chr17:8295358-8295538 | Common:1; Rare:46 | ||||
| chr17:8435706-8436034 | Common:4; Rare:125 | ||||
| chr17:10697409-10697648 | Common:3; Rare:106; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:11997444-11997602 | Rare:53 | ||||
| chr17:13601885-13602184 | Common:3; Rare:93 | ||||
| chr17:14069395-14069569 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:14300773-14301105 | Common:2; Rare:88 | ||||
| chr17:15262482-15262668 | Rare:45 | ||||
| chr17:15699497-15699773 | Common:3; Rare:72 | ||||
| chr17:15999591-15999776 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:16380687-16380814 | Common:2; Rare:26 | ||||
| chr17:16415538-16415824 | Common:4; Rare:75 | ||||
| chr17:17281182-17281337 | Rare:66 |